PC,

First of all, ALWAYS use a double boiler when heating glycerin,
no matter what other fractions it may contain. Second, ALWAYS use
slow and low heating techniques when heating glycerin, to reduce
the possibility of glycerin decaying to acrolein (extremely
toxic). Third,  NEVER use an open flame heat source when boiling
off alcohol, whether it's in the manufacture of glass soap or
anything else.

Whether or not you boiled the inordinate majority of alcohol off
is difficult to say. You will need a temperature several more
degrees above the boiling point of MeOH than the160* you
mentioned to achieve this, 165-170 sustained until all evidence
of boiling has ended.

It should be asked here if what you are referring to as
"glycerin" is recovered neutralized glycerin (from the process
where FFAs and catalyst are recovered as well) or the crude
glycerin layer prior to catalyst recovery, still containing the
FFAs and catalyst. In either event, you will need to calculate
backwards what the fractions are of the feedstock.

If the feedstock is neutralized recovered glycerin, the two
fractions will be H20 and glycerin (after the alcohol has been
evaporated). You can approximate the percentage of feedstock
purity by graphing the ratio weights of H20/glycerin and
comparing the per gallon weight of the feedstock to the graph.
From there you can determine where to add or subtract water from
other parts of the soap recipe that you are using.

If the feedstock you are referring to as glycerin is the
un-neutralized crude glycerin layer that settles out of a
transesterification reaction, you have an entirely different slew
of variables. (If you are using crude glycerin from WVO, it is
doubtful that you will be terribly pleased with the resulting
fragrance of your finished soap product.)

The crude glycerin will have fractions of FFAs, glycerin and
caustic (after the alcohol has been evaporated). You can presume
that the catalyst fraction is the same as what was initially
added to the methanol in the biodiesel process. It will actually
be slightly less. You can then use that information to calculate
necessary addition or subtraction of catalyst to match the soap
recipe's requirements.

You can roughly calculate the glycerin fraction to be ~79
milliliters for every liter of oil processed.procedure. The
balance of the crude glycerin layer will be FFAs, which can be
roughly considered the same as a base oil. (If you want to get
"critical," subtract 0.40 ml from the initial volume for every
gram of catalyst deemed to be present in the crude glycerin when
calculating what fractions of the crude glycerin are FFAs and
glycerin.)

You will need to balance how much of the crude glycerin layer you
add to any soap recipe. The volume will be limited by how much
catalyst, base oil and/or glycerin is called for.

If you choose to incorporate the use of biodiesel co-products
into your soap making, it will be helpful to log the inputs and
co-products for each batch and keep the co-products from
different batches labeled and separate from each other. This will
make these crude forms of back measuring  considerably more
accurate than just "guesswork," yielding more consistent results
in your soap manufacturing.

Todd Swearingen

----- Original Message -----
From: pcooke04102 <[EMAIL PROTECTED]>
To: <biofuel@yahoogroups.com>
Sent: Monday, August 26, 2002 9:00 AM
Subject: [biofuel] boiling glycerine/soap


> Here is a qustion for soap makers. I am trying to make soap out
of
> the waste glycerine. I boiled 2 liters glycerine at 160 degrees
F for
> about 15 minutes. Is this enough time to evaporate all the
methanol
> out? How do you know when its been evaporated.
> I then combined 50 grams of lye/liter of glycerine when both
were at
> temps around 100 degrees F and poured into the bottom of a
plastic
> jug. Looks like I have round disk of soap. I think I'll try
adding
> fragrance to the next batch to see if its workable, just
wondering
> about the methanol being gone-which I'm assuming it is. Any
comments
> or suggestions? Thanks in advance-PC
>
>
>
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